JPS61221242A - Low heat generating rubber composition - Google Patents
Low heat generating rubber compositionInfo
- Publication number
- JPS61221242A JPS61221242A JP6076085A JP6076085A JPS61221242A JP S61221242 A JPS61221242 A JP S61221242A JP 6076085 A JP6076085 A JP 6076085A JP 6076085 A JP6076085 A JP 6076085A JP S61221242 A JPS61221242 A JP S61221242A
- Authority
- JP
- Japan
- Prior art keywords
- rubber
- rubber composition
- weight
- low heat
- parts
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明は低発熱性ゴム組成物、特に詳しくは耐磨耗性等
を損うことなく発熱性を改善した低発熱性ゴム組成物に
関する。DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a low heat build-up rubber composition, and more particularly to a low heat build-up rubber composition that has improved heat build-up without impairing abrasion resistance.
(従来の技術)
省資源、省エネルギーの社会的要求に対応するため、ゴ
ム業界特にタイヤ東金において、ここ数年来、低燃費タ
イヤの開発が盛んに行われるようになってきた。このよ
うな低燃費タイヤの開発には低発熱性ゴム組成物が不可
欠であり、例えば、特に乗用車用タイヤを目的として、
特開昭57−51508号公報、特開昭57−5520
4.号公報、特開昭58−86705号公報に記載され
ているように、結合スチレンとビニル結合の含有基をコ
ントロールしたスチレン−ブタジェンゴム(SBR)ヲ
使用する方法があるが、これらの方法はSBR以外のゴ
ム、特に重車両用タイヤにもつとも広く使用されている
天然ゴムには全く応用できなかった。(Prior Art) In response to social demands for resource and energy conservation, the rubber industry, particularly Tire Togane, has been actively developing fuel-efficient tires over the past few years. Low heat generation rubber compositions are essential for the development of such fuel-efficient tires.For example, especially for passenger car tires,
JP-A-57-51508, JP-A-57-5520
4. As described in Japanese Patent Application Laid-Open No. 58-86705, there is a method of using styrene-butadiene rubber (SBR) in which the groups containing bonded styrene and vinyl bonds are controlled, but these methods do not apply to SBR. It could not be applied at all to natural rubber, which is widely used in tires for heavy vehicles, especially natural rubber.
一方、特公昭50−88181号公報、英国特許$E1
185896E明細書、米国特許第2815856号明
細書及び米国特許第2815856号明細書等にニトロ
ソキノリン類、ニトロソアニリン類等を添加することに
より、ゴム組成物の発熱性が改善されることが記載され
る。しかしながら、このようなニトロソ化合物は、確か
に発熱性は改善するが、特にポリイソプレンゴムに適用
した場合、ポリマーのしやく解作用が大きく、ゴム組成
物の耐磨耗性を著しく低下させるといった欠点を有して
いた。On the other hand, Japanese Patent Publication No. 50-88181, British Patent $E1
185896E, U.S. Pat. No. 2,815,856, U.S. Pat. No. 2,815,856, etc., it is described that the heat generation properties of rubber compositions are improved by adding nitrosoquinolines, nitrosoanilines, etc. . However, although such nitroso compounds do improve heat generation properties, they have the disadvantage that, especially when applied to polyisoprene rubber, they have a large decomposition effect on the polymer, significantly reducing the abrasion resistance of the rubber composition. It had
(発明が解決しようとする問題点)
本発明は、前記のような天然ゴムに応用することができ
なかったり、ポリイソプレンゴムに適用した場合、しや
く解作用が大きかったり、ゴム組成物の耐磨耗性を著し
く低下させたりする問題を解決して、このような欠点の
ない低発熱性ゴム組成物を提供しようとする。(Problems to be Solved by the Invention) The present invention cannot be applied to natural rubber as described above, or when applied to polyisoprene rubber, the disintegration effect is large or the rubber composition has a high resistance. An attempt is made to solve the problem of significantly lowering abrasion properties and provide a low heat build-up rubber composition that does not have such drawbacks.
(問題点を解決するための手段)
本発明者らは上記欠点を改善することを目的として、鋭
意検討した結果、アミノ酸がカーボンブラックと併用さ
れると、しやく解作用を示さず、かつ発熱を改善するこ
とを確め本発明に到達したものである。すなわち、本発
明の構成とするところは、天然ゴム及び/又はジエン系
合成ゴムからなるゴム100重量部に、カーボンブラッ
クを30〜150重量部、アミノ酸を0.1〜5fl量
部配合してなる低発熱性ゴム組成物である。(Means for Solving the Problems) The present inventors have conducted extensive studies with the aim of improving the above-mentioned drawbacks, and have found that when amino acids are used in combination with carbon black, they do not quickly decompose and do not generate heat. The present invention was developed by confirming that the present invention can improve the following. That is, the structure of the present invention is made by blending 30 to 150 parts by weight of carbon black and 0.1 to 5 fl parts of amino acids with 100 parts by weight of rubber made of natural rubber and/or diene-based synthetic rubber. It is a low heat generation rubber composition.
本発明において使用するゴムとしては、天然ゴム、合成
ポリイソプレンゴム、スチレン−ブタジェンゴム、ポリ
ブタジェンゴム、ブチルゴム等であり、これらのゴムを
単独もしくは2種以上併用することができる。Rubbers used in the present invention include natural rubber, synthetic polyisoprene rubber, styrene-butadiene rubber, polybutadiene rubber, butyl rubber, and these rubbers can be used alone or in combination of two or more.
本発明において使用するアミノ酸は、シスチン、リシン
、アルギニン、オキシリシン、グルタミン、アスパラギ
ン酸、グルタミン酸、セリン、グリシン、トレオニン、
アラニン、チロシン、トリプトファン、バリン、aイシ
ン、イソロイシン、ヒスチジン、α−フェニルアラニン
、プロリン、メチオニン等があり、好ましくはシスチン
、リシン、アルギニン、オキシリシン、グルタミン、ト
リプトファンなどであり、これらのアミノ酸を単独もし
くは21/@以上併用することができる。また、アミノ
酸の配合量は、ゴム100重量部に対して0.1〜5重
量部である。0.1 fE量郡部未満はゴム組成物の発
熱改良効果がほとんどなく、5重量部を越えると、もは
や増量効果がなくなるばかりでなく、ゴム組成物の機械
的性質が低下する。Amino acids used in the present invention include cystine, lysine, arginine, oxylysine, glutamine, aspartic acid, glutamic acid, serine, glycine, threonine,
These amino acids include alanine, tyrosine, tryptophan, valine, a-isine, isoleucine, histidine, α-phenylalanine, proline, methionine, etc., and preferably cystine, lysine, arginine, oxylysine, glutamine, tryptophan, etc. /@ or more can be used together. Further, the blending amount of the amino acid is 0.1 to 5 parts by weight per 100 parts by weight of rubber. If the amount is less than 0.1 parts by weight, there will be little effect on improving the heat generation of the rubber composition, and if it exceeds 5 parts by weight, not only will there be no effect in increasing the amount, but the mechanical properties of the rubber composition will deteriorate.
本発明において、カーボンブラックの配合量は、30〜
150重量部であり、30重量部未満ではゴム組成物の
補強性が劣り、150重量部を越えると、発熱性が著し
く悪化するばかりでなく、耐磨耗性等の物性が著しく悪
化する。In the present invention, the blending amount of carbon black is 30 to
If the amount is less than 30 parts by weight, the reinforcing properties of the rubber composition will be poor, and if it exceeds 150 parts by weight, not only the heat generation properties will be significantly deteriorated, but also the physical properties such as abrasion resistance will be significantly deteriorated.
本発明においては、上記のカーボンブラックとアミノ酸
以外に、必要に応じて軟化剤、老化防止剤、加硫促進剤
、加硫促進助剤、加硫剤等の通常ゴム工業で使用される
配合剤を適宜配合することができる。In the present invention, in addition to the above-mentioned carbon black and amino acids, compounding agents commonly used in the rubber industry, such as softeners, anti-aging agents, vulcanization accelerators, vulcanization accelerators, and vulcanizing agents, are used as necessary. can be appropriately blended.
(実施例)
以下、本発明を実施例および比較例により詳細に説明す
る。(Examples) Hereinafter, the present invention will be explained in detail with reference to Examples and Comparative Examples.
実施例1〜8、比較例1−8
第1麦に示した配合内容による各種ゴム組成物をバンバ
リーミキサ−を用いて混練りして作成し、反発弾性、ゾ
ル分子量及び耐磨耗性について評価した。結果をIEI
表に示した。比較のため、比較例1としてアミノ酸を配
合しない場合、比較例2として5−ニトロン−8−ヒト
ミキシキノI)7ヲ配合した場合、比較例8としてN−
フェニル−p−ニトロソアニリンを配合した場合につい
ても同様に評価した。Examples 1 to 8, Comparative Example 1-8 Various rubber compositions with the formulation shown in the first barley were kneaded using a Banbury mixer and evaluated for impact resilience, sol molecular weight, and abrasion resistance. did. IEI results
Shown in the table. For comparison, Comparative Example 1 is a case in which no amino acid is blended, Comparative Example 2 is a case in which 5-nitrone-8-human-mixiquino I) 7 is blended, and Comparative Example 8 is a case in which N-
The case where phenyl-p-nitrosoaniline was blended was similarly evaluated.
なお、評価方法は以下の通りである。The evaluation method is as follows.
反発弾性:JISK6301に従って測定した。Repulsion elasticity: Measured according to JISK6301.
ゾル分子量;未加硫ゴム組成物をテトラヒドロフランに
浸漬し48時間後、カーボンゲル
を除去した残液にて、東洋曹達膜
Hlgh 5peed Liquid Chromat
ographHLO−3021を使用してゾル分の分子
量(へ)を測定した。Sol molecular weight: After 48 hours of immersing the unvulcanized rubber composition in tetrahydrofuran, the remaining liquid after removing the carbon gel was stained with Toyo Soda Membrane Hlgh 5peed Liquid Chromat.
The molecular weight of the sol fraction was measured using ographHLO-3021.
耐磨耗性;第1表に示した各種ゴム組成物をタイヤサイ
ズ1000R20のトラック・バス用ラジアルタイヤの
トレッド部に用
いて、50000kll走行後、浅溝を測定し、1鱈当
りの走行距離を求め、比較
例1を100として指数で表示した。Abrasion resistance: The various rubber compositions shown in Table 1 were used in the tread of a radial tire for trucks and buses with a tire size of 1000R20, and after running 50,000 kll, the shallow grooves were measured and the mileage per cod was calculated. It was calculated and expressed as an index with Comparative Example 1 set as 100.
値が大なる程良好である。The larger the value, the better.
第1表から明らかなように、比較例で示したニトロン化
合物はレジリエンス改良効果はすぐれているが、ポリマ
ーのしやく解効果が大きく、その結果耐磨耗性が低下す
るのに対し、アミノ噛を配合した本発明に係るゴム組成
物は、レジリエンス改良効果はニトロソ化合物と比較し
てやや劣るが、ポリマーのしやく解が#1とんどなく、
発熱性と耐磨耗性の両性能を同時に満足することが可能
である。As is clear from Table 1, the nitrone compound shown in the comparative example has an excellent resilience improvement effect, but the polymer has a large decomposition effect, resulting in a decrease in wear resistance, whereas the amino compound has an excellent effect on improving resilience. The rubber composition according to the present invention, which is blended with , has a slightly inferior resilience improvement effect compared to the nitroso compound, but it has a #1 polymer dissolution rate, and
It is possible to satisfy both properties of heat generation and wear resistance at the same time.
実施例9〜12、比較例4〜5
第2表に示す配合内容にて作成したゴム組成物について
、実施例1と同様に反発弾性と耐磨耗性を評価した。結
果を第2表に示す。Examples 9 to 12, Comparative Examples 4 to 5 Rubber compositions prepared with the formulations shown in Table 2 were evaluated for impact resilience and abrasion resistance in the same manner as in Example 1. The results are shown in Table 2.
*2表から、本発明のゴム組成物は発熱性と耐磨耗性の
両立が可能であることがわかる。*From Table 2, it can be seen that the rubber composition of the present invention is capable of achieving both heat generation properties and abrasion resistance.
第 2 表
本比較例番を100として指数表示
(発明の効果)
以上、実施例及び比較例から明らかなよ5に、本発明は
、天然ゴム及び/又はジエン系合成ゴムからなるゴムに
特定量のカーボンブラック及びアミノ酸を配合してなる
ゴム組成物を提供し、これによって、従来のようにしや
く解作用が大きかったり、ゴム組成物の耐磨耗性を著し
く低下させたりすることなく、低発熱性を実現すること
ができる。Table 2 Index display (effects of the invention) with the present comparative example number set as 100 As is clear from the above examples and comparative examples, the present invention applies The present invention provides a rubber composition containing carbon black and an amino acid, which generates low heat generation without increasing the quick decomposition effect or significantly reducing the abrasion resistance of the rubber composition as in the past. You can realize your sexuality.
Claims (1)
100重量部に、カーボンブラックを30〜150重量
部、アミノ酸を0.1〜5重量部配合したことを特徴と
する低発熱性ゴム組成物。 2、アミノ酸がシスチン、リシン、アルギニン、オキシ
リシン、グルタミン、アスパラギン酸、グルタミン酸、
セリン、グリシン、トレオニン、アラニン、チロシン、
トリプトファン、バリン、ロイシン、イソロイシン、ヒ
スチジン、α−フェニルアラニン、プロリン又はメチオ
ニンである特許請求の範囲第1項記載のゴム組成物。 3、アミノ酸がシスチン、リシン、アルギニン、オキシ
リシン、グルタミン又はトリプトファンである特許請求
の範囲第1項記載のゴム組成物。[Claims] 1. 100 parts by weight of rubber made of natural rubber and/or diene-based synthetic rubber is blended with 30 to 150 parts by weight of carbon black and 0.1 to 5 parts by weight of amino acids. Low heat generation rubber composition. 2. Amino acids are cystine, lysine, arginine, oxylysine, glutamine, aspartic acid, glutamic acid,
serine, glycine, threonine, alanine, tyrosine,
The rubber composition according to claim 1, wherein the rubber composition is tryptophan, valine, leucine, isoleucine, histidine, α-phenylalanine, proline, or methionine. 3. The rubber composition according to claim 1, wherein the amino acid is cystine, lysine, arginine, oxylysine, glutamine or tryptophan.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6076085A JPS61221242A (en) | 1985-03-27 | 1985-03-27 | Low heat generating rubber composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6076085A JPS61221242A (en) | 1985-03-27 | 1985-03-27 | Low heat generating rubber composition |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS61221242A true JPS61221242A (en) | 1986-10-01 |
Family
ID=13151551
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP6076085A Pending JPS61221242A (en) | 1985-03-27 | 1985-03-27 | Low heat generating rubber composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS61221242A (en) |
Cited By (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2003031510A1 (en) * | 2001-10-05 | 2003-04-17 | Bridgestone Corporation | Rubber composition |
JP2009019098A (en) * | 2007-07-11 | 2009-01-29 | Sumitomo Rubber Ind Ltd | Rubber composition for tire and pneumatic tire using the same |
JP2009019097A (en) * | 2007-07-11 | 2009-01-29 | Sumitomo Rubber Ind Ltd | Rubber composition for tire |
JP2009275180A (en) * | 2008-05-16 | 2009-11-26 | Yokohama Rubber Co Ltd:The | Rubber composition |
JP2012224685A (en) * | 2011-04-15 | 2012-11-15 | Yokohama Rubber Co Ltd:The | Rubber composition |
JP2013049811A (en) * | 2011-08-31 | 2013-03-14 | Sumitomo Rubber Ind Ltd | Rubber composition for tire and pneumatic tire |
JP2013107991A (en) * | 2011-11-21 | 2013-06-06 | Sumitomo Rubber Ind Ltd | Rubber composition for tire and pneumatic tire |
WO2013129394A1 (en) | 2012-03-02 | 2013-09-06 | 株式会社ブリヂストン | Rubber composition and method for producing rubber composition |
EP2639246A1 (en) * | 2012-03-14 | 2013-09-18 | The Goodyear Tire & Rubber Company | Functionalized elastomer and tire comprising such an elastomer |
EP2639245A1 (en) * | 2012-03-14 | 2013-09-18 | The Goodyear Tire & Rubber Company | Rubber composition and pneumatic tire |
JP2014077028A (en) * | 2012-10-09 | 2014-05-01 | Sumitomo Chemical Co Ltd | Method for producing rubber composition, vulcanized rubber composition molded product and vibration-proof material |
JP2014196385A (en) * | 2013-03-29 | 2014-10-16 | 横浜ゴム株式会社 | Rubber composition and pneumatic tire |
WO2016009776A1 (en) * | 2014-07-15 | 2016-01-21 | 住友ゴム工業株式会社 | Method for producing rubber composition for tires, and pneumatic tire |
JPWO2014119694A1 (en) * | 2013-01-30 | 2017-01-26 | 株式会社ブリヂストン | Rubber composition and pneumatic tire using the same |
WO2019002437A1 (en) * | 2017-06-29 | 2019-01-03 | Bridgestone Corporation | Rubber compounds for pneumatic tyres comprising recycled carbon black |
-
1985
- 1985-03-27 JP JP6076085A patent/JPS61221242A/en active Pending
Cited By (23)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2003031510A1 (en) * | 2001-10-05 | 2003-04-17 | Bridgestone Corporation | Rubber composition |
EP2223958A1 (en) * | 2001-10-05 | 2010-09-01 | Bridgestone Corporation | Rubber composition |
US7799856B2 (en) | 2001-10-05 | 2010-09-21 | Bridgestone Corporation | Rubber composition |
US8110625B2 (en) | 2001-10-05 | 2012-02-07 | Bridgestone Corporation | Rubber composition |
JP2009019098A (en) * | 2007-07-11 | 2009-01-29 | Sumitomo Rubber Ind Ltd | Rubber composition for tire and pneumatic tire using the same |
JP2009019097A (en) * | 2007-07-11 | 2009-01-29 | Sumitomo Rubber Ind Ltd | Rubber composition for tire |
JP2009275180A (en) * | 2008-05-16 | 2009-11-26 | Yokohama Rubber Co Ltd:The | Rubber composition |
JP2012224685A (en) * | 2011-04-15 | 2012-11-15 | Yokohama Rubber Co Ltd:The | Rubber composition |
JP2013049811A (en) * | 2011-08-31 | 2013-03-14 | Sumitomo Rubber Ind Ltd | Rubber composition for tire and pneumatic tire |
JP2013107991A (en) * | 2011-11-21 | 2013-06-06 | Sumitomo Rubber Ind Ltd | Rubber composition for tire and pneumatic tire |
WO2013129394A1 (en) | 2012-03-02 | 2013-09-06 | 株式会社ブリヂストン | Rubber composition and method for producing rubber composition |
US9518172B2 (en) | 2012-03-02 | 2016-12-13 | Bridgestone Corporation | Rubber composition and method for producing rubber composition |
EP2639246A1 (en) * | 2012-03-14 | 2013-09-18 | The Goodyear Tire & Rubber Company | Functionalized elastomer and tire comprising such an elastomer |
EP2639245A1 (en) * | 2012-03-14 | 2013-09-18 | The Goodyear Tire & Rubber Company | Rubber composition and pneumatic tire |
JP2014077028A (en) * | 2012-10-09 | 2014-05-01 | Sumitomo Chemical Co Ltd | Method for producing rubber composition, vulcanized rubber composition molded product and vibration-proof material |
JPWO2014119694A1 (en) * | 2013-01-30 | 2017-01-26 | 株式会社ブリヂストン | Rubber composition and pneumatic tire using the same |
US10053553B2 (en) | 2013-01-30 | 2018-08-21 | Bridgestone Corporation | Rubber composition, and pneumatic tire using same |
JP2014196385A (en) * | 2013-03-29 | 2014-10-16 | 横浜ゴム株式会社 | Rubber composition and pneumatic tire |
WO2016009776A1 (en) * | 2014-07-15 | 2016-01-21 | 住友ゴム工業株式会社 | Method for producing rubber composition for tires, and pneumatic tire |
JPWO2016009776A1 (en) * | 2014-07-15 | 2017-04-27 | 住友ゴム工業株式会社 | Manufacturing method of rubber composition for tire and pneumatic tire |
WO2019002437A1 (en) * | 2017-06-29 | 2019-01-03 | Bridgestone Corporation | Rubber compounds for pneumatic tyres comprising recycled carbon black |
CN110832024A (en) * | 2017-06-29 | 2020-02-21 | 株式会社普利司通 | Rubber compound for pneumatic tire containing regenerated carbon black |
JP2020523456A (en) * | 2017-06-29 | 2020-08-06 | 株式会社ブリヂストン | Rubber compound for pneumatic tires containing recycled carbon black |
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